Allele Registry

Canonical Allele Identifier: PA147281

Gene: FOXC1 HGNC NCBI

ClinVar Variation Id: 93747

ClinVar Variation Id: 1502495

ClinVar RCV Id: RCV002022370

HGVS (amino-acid)	Matching Registered Transcripts
NP_001444.2:p.Gly456dup	CA147280 NM_001453.3:c.1359_1361dup CA565356226 NM_001453.3:c.1362_1364dup CA2677060677 NM_001453.3:c.1361_1362insTGG CA2677060678 NM_001453.3:c.1361_1362insAGG CA2677060682 NM_001453.3:c.1365_1367dup